| Document Name | Type | Number | Download |
|---|---|---|---|
| E-Consent Certificate | As Indicated | F-140 | icon-doc |
| E-Consent at Quorum Review - Client Guidance | Guidance | G-215 | icon-pdf |
| Central Study Questionnaire | Required | F-013 | icon-doc |
| Device Study Submission Form | As Indicated | F-019 | icon-doc |
| Board Meeting Schedule | Guidance | F-025 | icon-pdf |
| Waiver of Documentation of Informed Consent Submission Form | As Indicated | F-042 | icon-doc |
| Waiver or Alteration of Informed Consent Submission Form | As Indicated | F-043 | icon-doc |
| Observational Registry Site Information Questionnaire | Required | F-101 | icon-doc |
| Client Guide to Consent Form Evaluation (Requires an OnQ Portal Account) | Guidance | G-034 | icon-aspx |
| Consenting Research Participant Guidelines | Guidance | G-035 | icon-doc |
| Consent Form Versioning Guidelines | Guidance | G-039 | icon-doc |
| Handbook for Quorum Review IRB (Requires an OnQ Portal Account) | Guidance | G-043 | icon-aspx |
| Central Study Submission Checklist | Guidance | G-091 | icon-doc |
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